A cystic fibrosis patient who is homozygous for the A559T mutation

Am J Hum Genet. 1995 Sep;57(3):734.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Cystic Fibrosis / genetics*
  • Female
  • Homozygote
  • Humans
  • Mutation*